Absence of p53 autoantibodies in a significant proportion of breast cancer patients.

We analysed antibodies specific for human p53 in sera from primary breast cancer patients using three different immunoassays and we related these results to the p53 level in tumour tissue detected by immunohistochemistry. Only 44% (11/25) of apparently enzyme-linked immunosorbent assay (ELISA)-posit...

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Main Authors: Vojtesek, B., Kovarik, J., Dolezalova, H., Nenutil, R., Havlis, P., Brentani, R. R., Lane, D. P.
Format: Online
Language:English
Published: 1995
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033849/
id pubmed-2033849
recordtype oai_dc
spelling pubmed-20338492009-09-10 Absence of p53 autoantibodies in a significant proportion of breast cancer patients. Vojtesek, B. Kovarik, J. Dolezalova, H. Nenutil, R. Havlis, P. Brentani, R. R. Lane, D. P. Research Article We analysed antibodies specific for human p53 in sera from primary breast cancer patients using three different immunoassays and we related these results to the p53 level in tumour tissue detected by immunohistochemistry. Only 44% (11/25) of apparently enzyme-linked immunosorbent assay (ELISA)-positive sera were from patients with a high level of p53 protein in more than 50% of their tumour cells. Surprisingly, 36% (9/25) of the sera originated from patients with no detectable p53 protein at all. Immunoprecipitation data suggested that the reason for this discrepancy is that at least some of the antibodies detected as positive in the ELISA in these sera from patients with clinical stage I and stage II breast cancers may be induced by immunogens other than p53 protein. Many of these reactions give apparently positive signals in a variety of p53 assays, and very stringent analysis is required to avoid possible misinterpretation of these responses as a p53-specific B-cell response in human cancer patients. 1995-06 /pmc/articles/PMC2033849/ /pubmed/7779720 Text en
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Vojtesek, B.
Kovarik, J.
Dolezalova, H.
Nenutil, R.
Havlis, P.
Brentani, R. R.
Lane, D. P.
spellingShingle Vojtesek, B.
Kovarik, J.
Dolezalova, H.
Nenutil, R.
Havlis, P.
Brentani, R. R.
Lane, D. P.
Absence of p53 autoantibodies in a significant proportion of breast cancer patients.
author_facet Vojtesek, B.
Kovarik, J.
Dolezalova, H.
Nenutil, R.
Havlis, P.
Brentani, R. R.
Lane, D. P.
author_sort Vojtesek, B.
title Absence of p53 autoantibodies in a significant proportion of breast cancer patients.
title_short Absence of p53 autoantibodies in a significant proportion of breast cancer patients.
title_full Absence of p53 autoantibodies in a significant proportion of breast cancer patients.
title_fullStr Absence of p53 autoantibodies in a significant proportion of breast cancer patients.
title_full_unstemmed Absence of p53 autoantibodies in a significant proportion of breast cancer patients.
title_sort absence of p53 autoantibodies in a significant proportion of breast cancer patients.
description We analysed antibodies specific for human p53 in sera from primary breast cancer patients using three different immunoassays and we related these results to the p53 level in tumour tissue detected by immunohistochemistry. Only 44% (11/25) of apparently enzyme-linked immunosorbent assay (ELISA)-positive sera were from patients with a high level of p53 protein in more than 50% of their tumour cells. Surprisingly, 36% (9/25) of the sera originated from patients with no detectable p53 protein at all. Immunoprecipitation data suggested that the reason for this discrepancy is that at least some of the antibodies detected as positive in the ELISA in these sera from patients with clinical stage I and stage II breast cancers may be induced by immunogens other than p53 protein. Many of these reactions give apparently positive signals in a variety of p53 assays, and very stringent analysis is required to avoid possible misinterpretation of these responses as a p53-specific B-cell response in human cancer patients.
publishDate 1995
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033849/
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